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CID 192540

group of stereoisomers with the chemical formula C₃₂H₃₉NO₁₀
ChemicalSubstance group_of_stereoisomers Q82910136
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CID 192540

Summary

CID 192540 is a group of stereoisomers[1].

Key Facts

  • CID 192540's instance of is recorded as group of stereoisomers[2].
  • CID 192540's CAS Registry Number is recorded as 151519-45-8[3].
  • CID 192540's canonical SMILES is recorded as O=C1OC(=CC=2OC3(C)CCC4C(C)(CCC(OC(=O)C)C4(COC(=O)C)COC(=O)CC)C3C(O)C12)C=5C=NC=CC5[4].
  • CID 192540's InChI is recorded as InChI=1S/C32H39NO10/c1-6-25(36)40-17-32(16-39-18(2)34)23-9-12-31(5)28(30(23,4)11-10-24(32)41-19(3)35)27(37)26-22(43-31)14-21(42-29(26)38)20-8-7-13-33-15-20/h7-8,13-15,23-24,27-28,37H,6,9-12,16-17H2,1-5H3/t23-,24+,27+,28-,30+,31+,32?/m1/s1[5].
  • CID 192540's InChIKey is recorded as CHNDKXSVDUZFCZ-DNVGYTOISA-N[6].
  • CID 192540's chemical formula is recorded as C₃₂H₃₉NO₁₀[7].
  • CID 192540's subclass of is recorded as drimane sesquiterpenoid[8].
  • CID 192540's subclass of is recorded as alkaloid[9].
  • CID 192540's PubChem CID is recorded as 192540[10].
  • CID 192540's found in taxon is recorded as Aspergillus fumigatus[11].
  • CID 192540's isomeric SMILES is recorded as CCC(=O)OCC1(COC(C)=O)C@@HCC[C@]2(C)[C@H]3C@@Hc4c(cc(-c5cccnc5)oc4=O)O[C@@]3(C)CC[C@@H]12C@@HCC[C@]2(C)[C@H]3C@@Hc4c(cc(-c5cccnc5)oc4=O)O[C@@]3(C)CC[C@@H]12">[12].
  • CID 192540's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+597.257396448'}[13].
  • CID 192540's SureChEMBL ID is recorded as 29711386[14].
  • CID 192540's DSSTox substance ID is recorded as DTXSID00934275[15].
  • CID 192540's DSSTOX compound identifier is recorded as DTXCID901362927[16].
  • CID 192540's UniChem compound ID is recorded as 61937900[17].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . PubChem. Retrieved . wikidata.org.
  10. [11] ↑ . Pyripyropenes, highly potent inhibitors of acyl-CoA:cholesterol acyltransferase produced by Aspergillus fumigatus. wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). CID 192540. Retrieved May 3, 2026, from https://4ort.xyz/entity/cid-192540
MLA “CID 192540.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/cid-192540.
BibTeX @misc{4ortxyz_cid-192540_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{CID 192540}}, year = {2026}, url = {https://4ort.xyz/entity/cid-192540}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): CID 192540 — https://4ort.xyz/entity/cid-192540 (retrieved 2026-05-03)

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